The Learning Center

ASTCT & NMDP Sickle Cell Disease Webinar Series

This webinar series aired throughout the month of September 2021, in honor of Sickle Cell Awareness Month. This series highlights how to get patients to curative options, treating patients with sickle cell disease, and patients and caregiver experiences throughout the treatment process. Recordings and slides from the live webinars have been posted here for your easy viewing.

  • Contains 4 Component(s), Includes Credits

    This webinar aired on September 7 at 10 AM - 11 AM CT/11 AM - 12 PM ET. It is the first webinar in the new ASTCT & National Marrow Donor Program® (NMDP)/Be The Match®​ Sickle Cell Webinar Series, in honor of Sickle Cell Awareness month. This first webinar featured presentations from clinicians and patient speakers on the referral process for patients with sickle cell disease to curative options with transplant.

    This webinar aired on September 7 at 10 AM - 11 AM CT/11 AM - 12 PM ET. It is the first webinar in the new ASTCT & National Marrow Donor Program® (NMDP)/Be The Match® Sickle Cell Webinar Series, in honor of Sickle Cell Awareness month. This first webinar featured presentations from clinicians and patient speakers on the referral process for patients with sickle cell disease to curative options with transplant. Other topics include:

    - General principles of referral and consultation
    - Psychosocial supports for patients in the referral process
    - Successful education models from New Jersey that connect community hematology and oncology physicians and transplant specialists.

    This webinar will be moderated by Dr. Maryam Zia, and feature presentations by Ana Gordon, a referral coordinator at University of Illinois at Chicago, and Dr. Jennifer Krajewski, from Hackensack Meridian Health. Each webinar in this series will also highlight patient's lived experiences within each of the topics.

    There will be a short Q&A section at the end of the webinar, so be sure to register and submit any questions in advance that you would like answered during the webinar by emailing info@astct.org. This webinar will be recorded and the recording and slides will be posted 24-48 hours after the live event.

    Accreditation Statement: This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of The France Foundation and the American Society for Transplantation and Cellular Therapy (ASTCT). The France Foundation is accredited by the ACCME to provide continuing medical education for physicians.

    Overview 

    This webinar, the inaugural event in the ASTCT & National Marrow Donor Program® (NMDP)/Be The Match® Sickle Cell Webinar Series, was originally broadcast on September 7, 2023, coinciding with Sickle Cell Awareness month.  The session featured presentations by clinicians and patient speakers focusing on the referral process for patients with sickle cell disease to curative options with transplant. The topics covered included general principles of referral and consultation, psychosocial supports for patients during the referral process, and successful education models from New Jersey that facilitate connections between community hematology and oncology physicians and transplant specialists. Dr. Maryam Zia moderated the webinar, and the presenters included Ana Gordon, a referral coordinator at the University of Illinois at Chicago, and Dr. Jennifer Krajewski from Hackensack Meridian Health. Each webinar in this series will also showcase patient's lived experiences related to the topics discussed. This webinar was recorded and recently reviewed to extend CME accreditation.

    Release Date: 4/15/2024

    Expiration Date: 4/15/2025

    Estimated Time to Complete Activity: One hour

    Continuing Medical Education Information

    Statement of Need: The Sickle Cell Warriors Program at NMDP is a patient services program that assists in typing for patients, financial assistance, counseling, patient education and providing peer connections. The primary feedback from patients in the Sickle Cell Warrior Program is that #1 barrier to treatment is physicians. Patients report that they are not being told about all of their treatment options; regardless of disease severity, they should at least be made aware of various options, but often they are not. Many patients go to the Sickle Cell Warriors Program to enroll in a clinical trial for transplant, but this usually does not cover cost of HLA typing. In this case, the referring physician has not gone through the process of HLA typing, either because of misinformation or because the physician refuses to provide an order for typing simply because they don’t agree with patients physicians. This is a clear miscommunication between the community oncologists and transplant physicians. In surveys, transplant physicians identify a lack of awareness, lack of confidence, and reliance on outdated data from the referring physicians. These referring physicians in a similar survey reported that their primary reason for not communicating all treatment options was noncompliance in patients who they did not believe had the means to move forward with treatment. This illustrates a complex problem between the three groups (referring community physicians, transplant physicians, and the patients themselves) that this webinar series aims to address.

    Target Audience: This activity is intended for physicians, both referring physicians and transplant specialists, scientists, and other healthcare professionals who are part of the multidisciplinary team.

    Learning Objectives: Upon completion of this education activity, participants will be able to:

    1. Describe the general principles for referring patients with sickle cell disease to transplant consultations.
    2. Identify areas of strengths and gaps for patient’s psychosocial support throughout the referral, decision making, and transplant process.
    3. Recognize opportunities for further communication and peer education with community oncologists, hematologists and transplant physicians in order to increase rates of getting sickle cell patients to curative options.


    In support of improving patient care, this activity has been planned and implemented by The France Foundation (TFF),  the National Marrow Donor Program (NMDP), and the American Society for Transplantation and Cellular Therapy (ASTCT). The France Foundation is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.

    Credit Designation 
    Physicians

    The France Foundation designates this enduring activity for a maximum of 1.0 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.  

    Method of Participation/How to Receive Credit:
    There are no fees for participating and receiving credit for this activity. Successful completion is achieved by reviewing the CE information, completing the pre-test, completing the activity, and completing the post-test and evaluation form. A score of at least 75% on the posttest is required to successfully complete this activity. The participant may take the test until successfully passed.
    If you are requesting AMA credits or a certificate of participation, your certificate will be available for download. 

    Disclosure Policy:
    In accordance with the ACCME Standards for Integrity and Independence in Accredited Continuing Education, TFF, NMDP, and ASTCT require that individuals in a position to control the content of an educational activity disclose all relevant financial relationships with a commercial entity. TFF, NMDP, and ASTCT resolve all conflicts of interest to ensure independence, objectivity, balance, and scientific rigor in all their educational programs. Furthermore, TFF, NMDP, and ASTCT seek to verify that all scientific research referred to, reported, or used in a CME/CE activity conforms to the generally accepted standards of experimental design, data collection, and analysis. TFF, NMDP, and ASTCT are committed to providing learners with high-quality CME/CE activities that promote improvements in health care and not those of a commercial interest.

    Planning committee members, faculty, reviewers, and activity staff have disclosed the following relevant financial relationships. All relevant financial relationships listed have been mitigated.

    Name of Individual

     Role in Activity

    Name of Commercial Interest(s)

    Nature of Relationship(s)

    Mechanism(s) implemented to resolve conflict of interest

    Jennifer Krajewski, MD

    Faculty

     

    No relevant financial disclosures

     

    NA

     

    NA

    Ana Gordon, LCSW, OSW-C

    Faculty

    No relevant financial disclosures

    NA

    NA

    Samantha Watters, MPH (Planner)

    Planning Committee member

    No relevant financial disclosures

     

     

     Medical

    Planning Committee member, TFF Content Reviewer

    No relevant financial disclosures

    NA

    NA

    Miriam Giles

    Planning Committee member

    No relevant financial disclosures

    NA

    NA

    Heather Knight Tarbox

    Planning Committee member

    No relevant financial disclosures

    NA

    NA

    Commercial Supporter Disclosures
    No commercial support was provided for this webinar.

    Disclosure of Unlabeled Use: TFF, NMDP, and ASTCT require CME faculty (speakers) to disclose when products or procedures being discussed are off label, unlabeled, experimental, and/or investigational, and any limitations on the information that is presented, such as data that are preliminary, or that represent ongoing research, interim analyses, and/or unsupported opinion. Faculty in this activity may discuss information about pharmaceutical agents that is outside of US Food and Drug Administration approved labeling. This information is intended solely for continuing medical education and is not intended to promote off-label use of these medications. TFF, NMDP, and ASTCT do not recommend the use of any agent outside of the labeled indications. If you have questions, contact the Medical Affairs Department of the manufacturer for the most recent prescribing information.

    Disclaimer: TFF, NMDP, and ASTCT present this information for educational purposes only. The content is provided solely by faculty who have been selected because of recognized expertise in their field. Participants have the professional responsibility to ensure that products are prescribed and used appropriately on the basis of their own clinical judgment and accepted standards of care. TFF, NMDP, and ASTCT assume no liability for the information herein.

  • Contains 4 Component(s), Includes Credits

    Join us on September 15 at 12:30 - 1:30 PM CT/1:30 - 2:30 PM ET, for the second webinar in the new ASTCT & NMDP Sickle Cell Webinar Series, in honor of Sickle Cell Awareness month. This webinar will feature presentations from clinicians and patient speakers on the decision making process for sickle cell patients and transplant.

    Join us on September 15 at 12:30 - 1:30 PM CT/1:30 - 2:30 PM ET, for the second webinar in the new ASTCT & NMDP Sickle Cell Webinar Series, in honor of Sickle Cell Awareness month. This webinar will feature presentations from clinicians and patient speakers on the decision making process for sickle cell patients and transplant. Other topics include:

    - ASH Guidelines for BMT with Sickle Cell Disease
    - How to optimize patients for transplant
    - Patient selection criteria

    This webinar will be moderated by Dr. Folashade Otegbeye, and feature presentations by Dr. Santosh Saraf (UIC), and Dr. Mark Walters (UCSF). Each webinar in this series will also highlight patient's lived experiences within each of the topics.

    There will be a short Q&A section at the end of the webinar, so be sure to register and submit any questions in advance that you would like answered during the webinar by emailing info@astct.org. This webinar will be recorded and the recording and slides will be posted 24-48 hours after the live event.

    Accreditation Statement: This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of The France Foundation and the American Society for Transplantation and Cellular Therapy (ASTCT). The France Foundation is accredited by the ACCME to provide continuing medical education for physicians.

    Continuing Medical Education Information

    This activity is jointly provided by The France Foundation and the American Society for Transplantation and Cellular Therapy.                

    Statement of Need:

    The Sickle Cell Warriors Program at NMDP is a patient services program that assists in typing for patients, financial assistance, counseling, patient education and providing peer connections. The primary feedback from patients in the Sickle Cell Warrior Program is that #1 barrier to treatment is physicians. Patients report that they are not being told about all of their treatment options; regardless of disease severity, they should at least be made aware of various options, but often they are not. Many patients go to the Sickle Cell Warriors Program to enroll in a clinical trial for transplant, but this usually does not cover cost of HLA typing. In this case, the referring physician has not gone through the process of HLA typing, either because of misinformation or because the physician refuses to provide an order for typing simply because they don’t agree with patients physicians. This is a clear miscommunication between the community oncologists and transplant physicians. In surveys, transplant physicians identify a lack of awareness, lack of confidence, and reliance on outdated data from the referring physicians. These referring physicians in a similar survey reported that their primary reason for not communicating all treatment options was noncompliance in patients who they did not believe had the means to move forward with treatment. This illustrates a complex problem between the three groups (referring community physicians, transplant physicians, and the patients themselves) that this webinar series aims to address.

    Target Audience:

    This activity is intended for physicians, both referring physicians and transplant specialists, scientists, and other healthcare professionals who are part of the multidisciplinary team.

    Learning Objectives:

    Upon completion of this education activity, participants will be able to:


    1. Explain methods to optimize patients for transplant

    2. Identify the ASH Guidelines for BMT in Sickle Cell Disease

    3. Apply patient selection criteria to case studies.


    Accreditation Statement:

    This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of The France Foundation and the American Society for Transplantation and Cellular Therapy. The France Foundation is accredited by the ACCME to provide continuing medical education for physicians.  

    Credit Designation 

    Physicians

    The France Foundation designates this live activity for a maximum of 1.0 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.  

    Method of Participation/How to Receive Credit:

    1. Review the activity objectives and CME/CE information.
    2. Participate in the CME/CE activity.
    3. Complete the CME/CE evaluation form, which provides each participant with the opportunity to comment on how participating in the activity will affect their professional practice; the quality of the instructional process; the perception of enhanced professional effectiveness; the perception of commercial bias; and his/her views on future educational needs.
    4. If you are requesting educational credits or a certificate of participation, your certificate will be available for download.

    Disclosure Policy:

    In accordance with the ACCME Standards for Commercial Support, The France Foundation (TFF) and the American Society for Transplantation and Cellular Therapy (ASTCT) require that individuals in a position to control the content of an educational activity disclose all relevant financial relationships with any commercial interest. TFF and ASTCT resolve all conflicts of interest to ensure independence, objectivity, balance, and scientific rigor in all their educational programs. Furthermore, TFF and ASTCT seek to verify that all scientific research referred to, reported, or used in a CME/CE activity conforms to the generally accepted standards of experimental design, data collection, and analysis. TFF and ASTCT are committed to providing learners with high-quality CME/CE activities that promote improvements in health care and not those of a commercial interest.

    Activity Staff Disclosures:

    The planners, reviewers, editors, staff, CME committee, or other members at The France Foundation who control content have no relevant financial relationships to disclose.

    The planners, reviewers, editors, staff, CME committee, or other members at the American Society for Transplantation and Cellular Therapy who control content have no relevant financial relationships to disclose.

    Faculty Disclosures

    Faculty disclosures will be provided prior to the start of the activity.

    Commercial Supporter Disclosures

    No commercial support is provided for this webinar.

    Disclosure of Unlabeled Use:

    TFF and ASTCT require CME faculty (speakers) to disclose when products or procedures being discussed are off label, unlabeled, experimental, and/or investigational, and any limitations on the information that is presented, such as data that are preliminary, or that represent ongoing research, interim analyses, and/or unsupported opinion. Faculty in this activity may discuss information about pharmaceutical agents that is outside of US Food and Drug Administration approved labeling. This information is intended solely for continuing medical education and is not intended to promote off-label use of these medications. TFF and ASTCT do not recommend the use of any agent outside of the labeled indications. If you have questions, contact the Medical Affairs Department of the manufacturer for the most recent prescribing information.

    Disclaimer:

    The France Foundation and the American Society for Transplantation and Cellular Therapy present this information for educational purposes only. The content is provided solely by faculty who have been selected because of recognized expertise in their field. Participants have the professional responsibility to ensure that products are prescribed and used appropriately on the basis of their own clinical judgment and accepted standards of care. The France Foundation and the American Society for Transplantation and Cellular Therapy assume no liability for the information herein.

  • Contains 4 Component(s), Includes Credits

    Join us on September 20 at 1 PM CT, for the third webinar in the new ASTCT & NMDP Sickle Cell Webinar Series, in honor of Sickle Cell Awareness month. This webinar will feature presentations from clinicians and patient speakers on challenges to finding stem cell sources and other barriers that both physicians and patients face throughout the process.

    Join us on September 20 at 1 PM CT, for the third webinar in the new ASTCT & NMDP Sickle Cell Webinar Series, in honor of Sickle Cell Awareness month. This webinar will feature presentations from clinicians and patient speakers on challenges to finding stem cell sources and other barriers that both physicians and patients face throughout the process. Other topics include:

    - Socioeconomic Barriers
    - Physicians attitude and practice
    - NMDP's Sickle Cell Warriors Program
    - Information about clinical trials

    This webinar will be moderated by Anna DeSalvo, a Senior Clinical Trials Patient Navigator with the NMDP Sickle Cell Warriors Program, and feature presentations by Dr. Lakshmanan Krishnamurti of Emory University. Each webinar in this series will also highlight patient's lived experiences within each of the topics.

    There will be a short Q&A section at the end of the webinar, so be sure to register and submit any questions in advance that you would like answered during the webinar by emailing info@astct.org. This webinar will be recorded and the recording and slides will be posted 24-48 hours after the live event.

    Accreditation Statement: This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of The France Foundation and the American Society for Transplantation and Cellular Therapy (ASTCT). The France Foundation is accredited by the ACCME to provide continuing medical education for physicians.

    Continuing Medical Education Information

    This activity is jointly provided by The France Foundation and the American Society for Transplantation and Cellular Therapy.                

    Statement of Need:

    The Sickle Cell Warriors Program at NMDP is a patient services program that assists in typing for patients, financial assistance, counseling, patient education and providing peer connections. The primary feedback from patients in the Sickle Cell Warrior Program is that #1 barrier to treatment is physicians. Patients report that they are not being told about all of their treatment options; regardless of disease severity, they should at least be made aware of various options, but often they are not. Many patients go to the Sickle Cell Warriors Program to enroll in a clinical trial for transplant, but this usually does not cover cost of HLA typing. In this case, the referring physician has not gone through the process of HLA typing, either because of misinformation or because the physician refuses to provide an order for typing simply because they don’t agree with patients physicians. This is a clear miscommunication between the community oncologists and transplant physicians. In surveys, transplant physicians identify a lack of awareness, lack of confidence, and reliance on outdated data from the referring physicians. These referring physicians in a similar survey reported that their primary reason for not communicating all treatment options was noncompliance in patients who they did not believe had the means to move forward with treatment. This illustrates a complex problem between the three groups (referring community physicians, transplant physicians, and the patients themselves) that this webinar series aims to address.

    Target Audience:

    This activity is intended for physicians, both referring physicians and transplant specialists, scientists, and other healthcare professionals who are part of the multidisciplinary team.

    Learning Objectives:

    Upon completion of this education activity, participants will be able to:

    1. Review potential challenges in finding an appropriate stem cell source, and enrolling in clinical trials.

    2. Identify potential socioeconomic barriers for patients in the transplant process, and relevant supports and programs to alleviate potential barriers and burdens.

    3. Examine any underlying hesitancy in colleagues in the field, to help engage colleagues in a meaningful way throughout the transplant process.

    Accreditation Statement:

    This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of The France Foundation and the American Society for Transplantation and Cellular Therapy. The France Foundation is accredited by the ACCME to provide continuing medical education for physicians.  

    Credit Designation 

    Physicians

    The France Foundation designates this live activity for a maximum of 1.0 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.  

    Method of Participation/How to Receive Credit:

    1. Review the activity objectives and CME/CE information.
    2. Participate in the CME/CE activity.
    3. Complete the CME/CE evaluation form, which provides each participant with the opportunity to comment on how participating in the activity will affect their professional practice; the quality of the instructional process; the perception of enhanced professional effectiveness; the perception of commercial bias; and his/her views on future educational needs.
    4. If you are requesting educational credits or a certificate of participation, your certificate will be available for download.

    Disclosure Policy:

    In accordance with the ACCME Standards for Commercial Support, The France Foundation (TFF) and the American Society for Transplantation and Cellular Therapy (ASTCT) require that individuals in a position to control the content of an educational activity disclose all relevant financial relationships with any commercial interest. TFF and ASTCT resolve all conflicts of interest to ensure independence, objectivity, balance, and scientific rigor in all their educational programs. Furthermore, TFF and ASTCT seek to verify that all scientific research referred to, reported, or used in a CME/CE activity conforms to the generally accepted standards of experimental design, data collection, and analysis. TFF and ASTCT are committed to providing learners with high-quality CME/CE activities that promote improvements in health care and not those of a commercial interest.

    Activity Staff Disclosures:

    The planners, reviewers, editors, staff, CME committee, or other members at The France Foundation who control content have no relevant financial relationships to disclose.

    The planners, reviewers, editors, staff, CME committee, or other members at the American Society for Transplantation and Cellular Therapy who control content have no relevant financial relationships to disclose.

    Faculty Disclosures

    Faculty disclosures will be provided prior to the start of the activity.

    Commercial Supporter Disclosures

    No commercial support is provided for this webinar.

    Disclosure of Unlabeled Use:

    TFF and ASTCT require CME faculty (speakers) to disclose when products or procedures being discussed are off label, unlabeled, experimental, and/or investigational, and any limitations on the information that is presented, such as data that are preliminary, or that represent ongoing research, interim analyses, and/or unsupported opinion. Faculty in this activity may discuss information about pharmaceutical agents that is outside of US Food and Drug Administration approved labeling. This information is intended solely for continuing medical education and is not intended to promote off-label use of these medications. TFF and ASTCT do not recommend the use of any agent outside of the labeled indications. If you have questions, contact the Medical Affairs Department of the manufacturer for the most recent prescribing information.

    Disclaimer:

    The France Foundation and the American Society for Transplantation and Cellular Therapy present this information for educational purposes only. The content is provided solely by faculty who have been selected because of recognized expertise in their field. Participants have the professional responsibility to ensure that products are prescribed and used appropriately on the basis of their own clinical judgment and accepted standards of care. The France Foundation and the American Society for Transplantation and Cellular Therapy assume no liability for the information herein.

  • Contains 4 Component(s), Includes Credits

    Join us on September 29 at 12 PM CT, for the fourth and final webinar in the new ASTCT & NMDP Sickle Cell Webinar Series, in honor of Sickle Cell Awareness month. This webinar will feature presentations from clinicians and patient speakers on guidelines for post-transplant care and updated CIBMTR outcomes data.

    Join us on September 29 at 12 PM CT, for the fourth and final webinar in the new ASTCT & NMDP Sickle Cell Webinar Series, in honor of Sickle Cell Awareness month. This webinar will feature presentations from clinicians and patient speakers on guidelines for post-transplant care and updated CIBMTR outcomes data. Other topics include:

    - Expectations for organ function and recovery
    - Ongoing psychosocial supports for patients and their families
    - Updated outcomes data from CIBMTR, including: overall survival and subsequent cancers after transplant

    This webinar will be moderated by Dr. Rachel Phelan, and feature presentations by Dr. Mary Eapen from the Medical College of Wisconsin, and Dr. Elizabeth Stenger from UPMC Children's Hospital of Pittsburgh. Each webinar in this series will also highlight patient's lived experiences within each of the topics.

    There will be a short Q&A section at the end of the webinar, so be sure to register and submit any questions in advance that you would like answered during the webinar by emailing info@astct.org. This webinar will be recorded and the recording and slides will be posted 24-48 hours after the live event.

    Accreditation Statement: This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of The France Foundation and the American Society for Transplantation and Cellular Therapy (ASTCT). The France Foundation is accredited by the ACCME to provide continuing medical education for physicians.

    Continuing Medical Education Information

    This activity is jointly provided by The France Foundation and the American Society for Transplantation and Cellular Therapy.                

    Statement of Need:

    The Sickle Cell Warriors Program at NMDP is a patient services program that assists in typing for patients, financial assistance, counseling, patient education and providing peer connections. The primary feedback from patients in the Sickle Cell Warrior Program is that #1 barrier to treatment is physicians. Patients report that they are not being told about all of their treatment options; regardless of disease severity, they should at least be made aware of various options, but often they are not. Many patients go to the Sickle Cell Warriors Program to enroll in a clinical trial for transplant, but this usually does not cover cost of HLA typing. In this case, the referring physician has not gone through the process of HLA typing, either because of misinformation or because the physician refuses to provide an order for typing simply because they don’t agree with patients physicians. This is a clear miscommunication between the community oncologists and transplant physicians. In surveys, transplant physicians identify a lack of awareness, lack of confidence, and reliance on outdated data from the referring physicians. These referring physicians in a similar survey reported that their primary reason for not communicating all treatment options was noncompliance in patients who they did not believe had the means to move forward with treatment. This illustrates a complex problem between the three groups (referring community physicians, transplant physicians, and the patients themselves) that this webinar series aims to address.

    Target Audience:

    This activity is intended for physicians, both referring physicians and transplant specialists, scientists, and other healthcare professionals who are part of the multidisciplinary team.

    Learning Objectives:

    Upon completion of this education activity, participants will be able to:

    1. Describe the long term psychosocial impacts in patients and their caregivers after transplant, and identify potential supports for long term survivorships.

    2. Define the general guidelines for post-transplant care in order to set expectations for patients in their recovery.

    3. Summarize trends in outcomes data, including rates of subsequent cancers after transplant.

    Accreditation Statement:

    This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of The France Foundation and the American Society for Transplantation and Cellular Therapy. The France Foundation is accredited by the ACCME to provide continuing medical education for physicians.  

    Credit Designation 

    Physicians

    The France Foundation designates this live activity for a maximum of 1.0 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.  

    Method of Participation/How to Receive Credit:

    1. Review the activity objectives and CME/CE information.
    2. Participate in the CME/CE activity.
    3. Complete the CME/CE evaluation form, which provides each participant with the opportunity to comment on how participating in the activity will affect their professional practice; the quality of the instructional process; the perception of enhanced professional effectiveness; the perception of commercial bias; and his/her views on future educational needs.
    4. If you are requesting educational credits or a certificate of participation, your certificate will be available for download.

    Disclosure Policy:

    In accordance with the ACCME Standards for Commercial Support, The France Foundation (TFF) and the American Society for Transplantation and Cellular Therapy (ASTCT) require that individuals in a position to control the content of an educational activity disclose all relevant financial relationships with any commercial interest. TFF and ASTCT resolve all conflicts of interest to ensure independence, objectivity, balance, and scientific rigor in all their educational programs. Furthermore, TFF and ASTCT seek to verify that all scientific research referred to, reported, or used in a CME/CE activity conforms to the generally accepted standards of experimental design, data collection, and analysis. TFF and ASTCT are committed to providing learners with high-quality CME/CE activities that promote improvements in health care and not those of a commercial interest.

    Activity Staff Disclosures:

    The planners, reviewers, editors, staff, CME committee, or other members at The France Foundation who control content have no relevant financial relationships to disclose.

    The planners, reviewers, editors, staff, CME committee, or other members at the American Society for Transplantation and Cellular Therapy who control content have no relevant financial relationships to disclose.

    Faculty Disclosures

    Faculty disclosures will be provided prior to the start of the activity.

    Commercial Supporter Disclosures

    No commercial support is provided for this webinar.

    Disclosure of Unlabeled Use:

    TFF and ASTCT require CME faculty (speakers) to disclose when products or procedures being discussed are off label, unlabeled, experimental, and/or investigational, and any limitations on the information that is presented, such as data that are preliminary, or that represent ongoing research, interim analyses, and/or unsupported opinion. Faculty in this activity may discuss information about pharmaceutical agents that is outside of US Food and Drug Administration approved labeling. This information is intended solely for continuing medical education and is not intended to promote off-label use of these medications. TFF and ASTCT do not recommend the use of any agent outside of the labeled indications. If you have questions, contact the Medical Affairs Department of the manufacturer for the most recent prescribing information.

    Disclaimer:

    The France Foundation and the American Society for Transplantation and Cellular Therapy present this information for educational purposes only. The content is provided solely by faculty who have been selected because of recognized expertise in their field. Participants have the professional responsibility to ensure that products are prescribed and used appropriately on the basis of their own clinical judgment and accepted standards of care. The France Foundation and the American Society for Transplantation and Cellular Therapy assume no liability for the information herein.